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Invitrogen
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Peptide sequence: AESGGSSGGA GGGGAFGAGP GPERPNSTAD KNGALKCTFS APSHSTSLLQ
Sequence homology: Dog: 86%; Human: 100%
KLHL26, part of the Kelch-like family member 26, is a protein-coding gene located on chromosome 19. It has been associated with various cellular functions due to its structural components, particularly the BTB/POZ domain at the N-terminus which spans about 115 amino acids. This domain plays crucial roles in forming E3 ubiquitin ligases by facilitating interactions with Cullin3 and enabling KLHL protein homodimerization. The significance of KLHL26 extends to its potential involvement in familial genetic conditions, as evidenced by the identification of a novel damaging variant, which was validated through Sanger sequencing in affected family members. Moreover, the Kelch motif within the KLHL proteins underlines their diverse roles in cellular morphology, gene expression regulation, and interaction with extracellular entities, including possible implications in actin binding and virus interactions post-infection.
仅用于科研。不用于诊断过程。未经明确授权不得转售。
蛋白别名: kelch-like 26; kelch-like family member 26; Kelch-like protein 26
基因别名: KLHL26
UniProt ID: (Human) Q53HC5
Entrez Gene ID: (Human) 55295